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通过留置的小脑延髓池导管监测神经递质氨基酸:两种暴发性肝衰竭啮齿动物模型的比较。

Monitoring of neurotransmitter amino acids by means of an indwelling cisterna magna catheter: a comparison of two rodent models of fulminant liver failure.

作者信息

Swain M S, Bergeron M, Audet R, Blei A T, Butterworth R F

机构信息

Laboratory of Neurochemistry, André-Viallet Clinical Research Center, Hôpital Saint-Luc, University of Montreal, Quebec, Canada.

出版信息

Hepatology. 1992 Oct;16(4):1028-35. doi: 10.1002/hep.1840160428.

Abstract

Alterations of brain and cerebrospinal fluid amino acids have consistently been described in human and experimental fulminant liver failure. To evaluate the significance of such changes in the pathogenesis of hepatic encephalopathy in fulminant liver failure, brain and cerebrospinal fluid amino acids (glutamate, aspartate, GABA, glycine, taurine) were measured at various stages during the development of neurological dysfunction in rats after hepatic devascularization or thioacetamide treatment to induce acute liver failure. To facilitate repetitive removal of cerebrospinal fluid, a technique employing long-term implantation of cisterna magna catheters in conscious, freely moving rats was developed. Brain but not cerebrospinal fluid concentrations of the excitatory amino acids glutamate and aspartate were reduced in both animal models of fulminant liver failure in parallel with deterioration of neurological status. Brain and cerebrospinal fluid GABA levels were not significantly altered. Cerebrospinal fluid glycine levels were increased two to three times in parallel with increasing brain glycine content in the devascularized rat but were unchanged in thioacetamide-induced liver failure, suggesting distinct pathophysiological mechanisms in these two experimental situations. On the other hand, onset of coma in both animal models of fulminant liver failure was accompanied by significantly increased cerebrospinal fluid taurine levels. We suggest that such changes result from taurine release from astrocytes in brain into the extracellular fluid; this is consistent with taurine's role in the regulation of intracellular osmolarity in brain. Sequential measurements of amino acids in the cerebrospinal fluid of small rodents with indwelling cisterna magna catheters adds a useful new approach for exploring the neurobiology of hepatic encephalopathy in fulminant liver failure.

摘要

在人类和实验性暴发性肝衰竭中,一直有关于脑和脑脊液氨基酸变化的描述。为了评估这些变化在暴发性肝衰竭肝性脑病发病机制中的意义,在肝去血管化或硫代乙酰胺处理诱导大鼠急性肝衰竭后,在神经功能障碍发展的不同阶段测量了脑和脑脊液中的氨基酸(谷氨酸、天冬氨酸、γ-氨基丁酸、甘氨酸、牛磺酸)。为便于重复采集脑脊液,开发了一种在清醒、自由活动的大鼠中长期植入枕大池导管的技术。在两种暴发性肝衰竭动物模型中,随着神经状态的恶化,兴奋性氨基酸谷氨酸和天冬氨酸的脑内浓度降低,但脑脊液中的浓度未降低。脑和脑脊液中的γ-氨基丁酸水平无明显改变。在去血管化大鼠中,脑脊液甘氨酸水平随着脑内甘氨酸含量的增加而升高两到三倍,但在硫代乙酰胺诱导的肝衰竭中未发生变化,这表明这两种实验情况下存在不同的病理生理机制。另一方面,两种暴发性肝衰竭动物模型中昏迷的发生都伴随着脑脊液牛磺酸水平的显著升高。我们认为这种变化是由于脑中星形胶质细胞释放牛磺酸进入细胞外液所致;这与牛磺酸在调节脑内细胞渗透压方面的作用是一致的。通过长期植入枕大池导管对小型啮齿动物脑脊液中的氨基酸进行连续测量,为探索暴发性肝衰竭肝性脑病的神经生物学提供了一种有用的新方法。

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